LubriFresh P.M. description, usages, side effects, indications, overdosage, supplying and lots more!

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LubriFresh P.M.

Major Pharaceuticals
Bausch & Lomb Incorporated

Artificial Tears Ointment Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Mineral oil 15%
White petrolatum 83%

Purpose

Lubricant

LubriFresh P.M. Uses

  • to prevent further irritation
  • to relieve dryness of the eye

Warnings

When using this product  

  • replace cap after use
  • do not touch tip of container to any surface to avoid contamination

Stop use and ask a doctor if

  • condition worsens or persists for more than 72 hours
  • you experience eye pain, changes in vision, continued redness or irritation of the eye

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  •  pull down the lower lid of the affected eye (s)
  •  apply a small amount (1/4 inch) of ointment to the inside of eyelid
  •  apply one or more times daily or as directed by a doctor

LubriFresh P.M. Other information

  • store at 15° - 30°C (59° - 86°F)
  • keep tightly closed
  • see crimp of tube or carton for Lot Number and Expiration Date

 

Inactive ingredient

lanolin oil

Questions or comments?

Serious side effects associated with use of this product may be reported to 1800-323-0000

*Major LubriFreshTM P.M. is not manufactured or distributed by Allergan Inc., distributor of Refresh P.M.®

Package/Label Principal Display Panel

LubriFresh P.M.

NDC 0904-5168-38

Major®

LubriFreshTM P.M.

Lubricant Eye Ointment (Sterile)

PRESERVATIVE FREE

Prevents Irritation and Relieves Dryness of the eye

Compare to Active Ingredients of Refresh P.M.®*

Net Wt. 1/8 oz (3.5 g)

LubriFresh P.M.

white petrolatum mineral oil OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-5168
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Mineral Oil 150 mg
petrolatum 830 mg

Inactive Ingredients

Ingredient Name Strength
LANOLIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0904-5168-38 3.5 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-12-09


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Be sure to consult your doctor before taking any medication!
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